A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10269



Internal ID15195843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:153330590..153368703hg38UCSC Ensembl
Outerchr1:153303066..153341179hg19UCSC Ensembl
Outerchr1:151569690..151607803hg18UCSC Ensembl
Outerchr1:150116139..150154252hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3838114
hg1938114
hg1838114
hg1738114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7184
Supporting Variants
SamplesNA18956
Known GenesPGLYRP4, S100A9
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv10269
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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